Pesticide composition delivery vehicles

ABSTRACT

Vehicles for delivery and release of pesticide compositions are provided. In one aspect, the delivery vehicle is a capsule configured to resist release of a pesticide composition before application of the capsule at a locus where pest control is desired. The capsule is further configured to degrade following application at the locus where pest control is desired to facilitate release of the pesticide composition. In one particular but non-limiting form, the capsule includes a shell wall including a relatively high Bloom strength gelatin material and a plasticizer material, and the pesticide composition includes a fumigant such as 1,3-dichloropropene. Further embodiments, forms, objects, features, advantages, aspects, and benefits shall become apparent from the description and drawings.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. patent applicationSer. No. 13/870,023 filed Apr. 25, 2013 which claims priority to U.S.Provisional Patent Application No. 61/640,392 filed Apr. 30, 2012, thecontents of which are incorporated herein by reference in theirentirety.

BACKGROUND

The present application relates to vehicles configured to deliver andrelease pesticide compositions in a controlled manner, and moreparticularly but not exclusively, to degradable capsules formed of agelatin material and encapsulating a pesticide composition.

Fields, groves, orchards and other plant growing environments can beinfested with various pests, non-limiting examples of which includesoil-borne plant pathogens and/or plant parasitic nematodes. When suchinfestations involve soil-borne plant pathogens and/or plant parasiticnematodes, soil fumigation is often the best or only economical methodof reducing these pest populations sufficiently to produce high qualityand high yielding plant crops, including for example fruits andvegetables. In one application technique, a fumigant in a liquid orvapor phase is injected into the soil through a delivery nozzle insertedinto the soil to a desired depth. When injected in a liquid phase, thefumigant converts to a gas that spreads out in the soil surrounding thesite of injection.

In most instances, the application of fumigants utilizing this techniqueyields acceptable control of targeted pests. However, it is not freefrom shortcomings and undesirable side effects. For example, one problemthat arises in connection with the use of this technique is exposure ofworkers to noxious and dangerous fumes. Another problem with thistechnique is that a significant portion of the volatile substances inthe fumigants commonly escape into the atmosphere. This is often due tothe inability to precisely control the dosage and/or release of thefumigant. In turn, ground level ozone is generated from the reaction ofthe volatile fumigant with nitrogen oxides in the troposphere, and itcan be harmful to respiratory systems of animals and damage sensitiveplants. It is also believed that volatile substances used in certainfumigants may play a role in global ozone depletion in the Earth's upperatmosphere, which is known to be associated with a variety of negativeconsequences.

To reduce the loss of fumigants into the atmosphere, and the resultingloss of fumigant efficacy, a covering material such as a polyethylenesheet or tarp is sometimes utilized to cover the soil after applicationof the fumigant. The polyethylene tarp, although not impervious togases, can reduce the dissipation rate of gases into the air, and thusprevent the depletion of the volatile fumigants by evaporation into theatmosphere. Nonetheless, covering the soil with these materials islabor-intensive, complicated and requires special application equipment,and workers are still exposed to noxious and dangerous fumes. Inaddition, the use of capsules which contain the fumigant and are appliedvia implantation into the soil has been advanced as an approach forovercoming the above identified shortcomings and undesirable sideeffects. However, even with these advances, controlling the release offumigant from the capsule is problematic. For example, in many cases thefumigant is untimely released, in whole or in part, during shipping,storage or other handling of the capsules. This leads to decreasedeffectiveness of the implanted capsules and also exposes workershandling the capsules to the fumigant. In addition, control of the timeand rate at which the fumigant is released following implantation of thecapsule into the soil is still inadequate, and ground level ozone canstill be present in some instances. Accordingly, there is a demand forfurther improvements in this area of technology.

SUMMARY

Vehicles for delivery and release of pesticide compositions areprovided. In one aspect, the delivery vehicle is a capsule configured toresist release of a pesticide composition before application of thecapsule at a locus where pest control is desired. The capsule is furtherconfigured to degrade following application at the locus where pestcontrol is desired to facilitate release of the pesticide composition.In one particular but non-limiting form, the capsule includes a shellwall including a relatively high Bloom strength gelatin material and aplasticizer material, and the pesticide composition includes a fumigantsuch as 1,3-dichloropropene.

In one embodiment, a capsule includes a shell wall encapsulating apesticide composition and including a gelatin material having a Bloomstrength in the range of 250 to 300 grams. The shell wall also includesa plasticizer composition, and the gelatin material and the plasticizercomposition are present at a ratio by weight between 2:1 and 4:1.

In another embodiment, a process includes positioning a capsule at alocus to control pests. The capsule includes a shell wall encapsulatinga pesticide composition and including a gelatin material having a Bloomstrength in the range of 250 to 300 grams. The shell wall also includesa plasticizer composition, and the gelatin material and the plasticizercomposition are present at a ratio by weight between 2:1 and 4:1. In oneform, the process also includes applying a protease enzyme dissolved inwater to the capsule before it is positioned at the locus.

In yet another embodiment, a capsule includes a shell wall including agelatin material and a plasticizer composition which includes a mixtureof sorbitol and mannitol. The capsule also includes a pesticidecomposition encapsulated by the shell wall. The pesticide compositionincludes a fumigant and a fumed silica material.

In still another embodiment, a capsule includes a shell wall which isformed by a gelatin composition and encapsulates a pesticidecomposition. The pesticide composition includes a fumigant, a fumedsilica material and a dialdehyde cross-linking agent.

In another embodiment, a process includes providing a first mixtureincluding a fumed silica material and 1,3-dichloropropene; providing asecond mixture including type-B gelatin and a plasticizer including amixture of sorbitol, mannitol and sorbitol anhydrides; and encapsulatingthe first mixture in the second mixture using a rotary die apparatus.

Other aspects include unique methods, systems, devices, kits,assemblies, equipment, and/or apparatus related to delivery and releaseof pesticide compositions.

Further aspects, embodiments, forms, features, benefits, objects, andadvantages shall become apparent from the detailed description andfigures provided herewith.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a perspective, partially exploded view of a capsule fordelivery of a pesticide composition.

FIG. 2 is a section view of the capsule of FIG. 1 and schematicallyillustrates a cross-linked portion of the capsule shell wall.

FIG. 3 is a graphical illustration of pesticide release from variouscapsules.

FIG. 4 is a graphical illustration of soil release profiles of apesticide from various capsules.

DETAILED DESCRIPTION OF REPRESENTATIVE EMBODIMENTS

For purposes of promoting an understanding of the principles of theinvention, reference will now be made to the embodiments illustrated inthe drawings and specific language will be used to describe the same. Itwill nevertheless be understood that no limitation of the scope of theinvention is thereby intended, such alterations and furthermodifications in the illustrated device, and such further applicationsof the principles of the invention as illustrated therein beingcontemplated as would normally occur to one skilled in the art to whichthe invention relates.

Vehicles for delivery and release of pesticide compositions areprovided. As used herein the term “pesticide” is intended to encompassherbicides, fungicides, insecticides and bactericides. Similarly,depending on the particular form of the pesticide composition, peststhat can be targeted by the disclosed delivery vehicles include insects,plant pathogens, weeds, molluscs, nematodes, and microbes. It should beappreciated however that the foregoing are merely non-limiting examples.

In one aspect, the delivery vehicle is a capsule configured to resistrelease of a pesticide composition before application of the capsule ata locus where pest control is desired. The capsule is further configuredto degrade following application at the locus where pest control isdesired to facilitate release of the pesticide composition. In certainforms, the capsule is also configured to control various aspects of therelease of the pesticide composition, including for example its time andrate of release. In one particular but non-limiting form, the capsuleincludes a shell wall including a relatively high Bloom strength gelatinmaterial and a plasticizer material, and the pesticide compositionincludes a fumigant such as 1,3-dichloropropene.

Turning now to FIG. 1, a partial cut away view of one non-limiting formof a capsule 10 including a pesticide composition 12 is illustrated.Capsule 10 includes an external shell wall 14 which surrounds andencapsulates pesticide composition 12. In the illustrated form, shellwall 14 provides capsule 10 with a tablet or pill shape such that it isgenerally cylindrically shaped with hemispherical ends. However, itshould be understood that different forms and shapes for capsule 10 areenvisioned. For example, capsule 10 may be circular, spherical, oval,oblong oval, square, rectangular, disc-shaped, football-shaped,puck-shaped, or rod-shaped, just to provide a few non-limitingpossibilities.

Shell wall 14 includes a gelatin material which may be selected from anyof a number suitable possibilities. More particularly, non-limitinggelatin materials which may be used for shell wall 14 include type-Agelatin which is derived from collagen by an acid pretreatment processand type-B gelatin which is derived from collagen by an alkalinepretreatment process. Exemplary collagen sources from which type-Agelatin and type-B gelatin can be obtained include fish, and bovine andporcine bones and hides. It is also contemplated that the gelatinmaterial included in shell wall 14 could have side chains which havebeen modified through succination, carboxymethylation,carboxyethylation, methylation, hydroxyethylation, or acetylation, justto provide a few examples. In addition, it should be appreciated thatshell wall 14 is not limited to the inclusion of a single type ofgelatin material.

A variety of different gel strengths for the gelatin material includedin shell wall 14 are possible. Gel strength may be measured using aBloom Gelometer, and measured values of Bloom strength have units ofgrams and serve as relative indicators of the strength of a gel as afunction of resistance of the gel to penetration by a probe. One testprocedure for determining Bloom strength is disclosed in Industrial andEngineering Chemistry, Analytical Edition, Volume II, Page 348. In oneform, the gelatin material of shell wall 14 has a Bloom strength that isgreater than 200 grams. In another form, the gelatin material of shellwall 14 has a Bloom strength in the range of 220 to 300 grams. Inanother form, the gelatin material of shell wall 14 has a Bloom strengthin the range of 250 to 300 grams. In still another form, the gelatinmaterial of shell wall 14 has a Bloom strength in the range of 270 to300 grams. However, it should be appreciated that alternative values forthe Bloom strength of the gelatin material of shall wall 14 are possibleand contemplated.

In one particular form, shell wall 14 may only include the gelatinmaterial. However, in other forms shell wall 14 includes one or morematerials in addition to the gelatin material. In these forms, thegelatin material may be present in the range of 40%-90% by weight basedon the total weight of shell wall 14. In another form, the gelatinmaterial is present in the range of 50%-80% by weight based on the totalweight of shell wall 14. In yet another form, the gelatin material ispresent in the range of 60%-70% based on the total weight of shell wall14. It should be understood however that other values for the amount ofthe gelatin material included in shell wall 14 are contemplated.

Materials in shell wall 14 in addition to the gelatin material may bepresent to provide desired capsule forming properties and/or to modifyvarious properties of capsule 10. For example, the additionalmaterial(s) may alter capsule elasticity or degradation profiles ofshell wall 14, or increase capsule stability by, for example, enhancingthermal stability, light stability, and corrosion resistance. It shouldbe appreciated that the release profile of capsule 10 may be affected asa result of undertaking one or more of the above modifications to theproperties of capsule 10. Similarly, it should be understood that one ormore of these properties can be modified in order to provide capsule 10with release characteristics tailored for particular applications.

Non-limiting examples of additional materials that can be included inshell wall 14 include additional polymer materials, ultravioletabsorbents, preservatives, a plasticizer, a disintegrant to promotedegradation of capsule 10 and a cross-linking agent to stiffen thestructure of shell wall 14. More particular examples of additionalpolymer materials that can be included in shell wall 14 includepolyvinyl alcohol, polyethylene oxide, alginate, propylene and glycolalginate. Non-limiting examples of cross-linking agents that can beincluded in shell wall 14 are aldehydes such as glutaraldehyde, andstarch and starch derivatives can be used as disintegrants. Moreparticular examples of plasticizers that can be included in shell wall14 include corn syrup solids, polyethylene glycol, ethylene glycol,sucrose, mannitol, glycerol, fructose, sorbitol, cellulose,cyclodextrins, maltodextrins, dioctyl-sodium sulfosuccinate, triethylcitrate, tributyl citrate, 1,2-propylenglycol, mono-, di- or triacetatesof glycerol, natural gums or the like as well as mixtures of theforegoing.

In one particular but non-limiting form, shell wall 14 includes aplasticizer in addition to the gelatin material, and the plasticizer isa composition including a mixture of sorbitol, mannitol, and sorbitolanhydrides. One particular form of this type of plasticizer is availablecommercially from SP1 Pharma (Wilmington, Del.) as Sorbitol Special™.When shell wall 14 includes the gelatin material and a plasticizer, theymay be present relative to one another at a ratio by weight between 1:1and 5:1. In another form, the gelatin material and the plasticizer arepresent at a ratio by weight between 2:1 and 4:1. In still another form,the gelatin material and the plasticizer are present at a ratio byweight between 3:1 and 3.5:1, although further variations in the ratioby weight between the gelatin material and the plasticizer are possible.

Pesticide composition 12 can be of any form suitable for release fromcapsule 10. In one particular but non-limiting form, pesticidecomposition 12 includes a fumigant. Fumigants are pesticides that have arelatively high vapor pressure and hence can exist as a gas insufficient concentrations to kill pests in soil or enclosed spaces. Thetoxicity of the fumigant is proportional to its concentration and theexposure time. They are characterized by a good capacity for diffusionand act by penetrating the pest's respiratory system or being absorbedthrough the pest's cuticle. Exemplary fumigants that can be included inpesticide composition 12, either alone or in any suitable combination,include trichloronitromethane, 1,2-dichloropropane, 1,3-dichloropropene,ethylene dibromide, and methyl bromide. In one particular butnon-limiting form, the fumigant includes 1,3-dichloropropene. Oneparticular form of this type of fumigant is available commercially fromDow AgroSciences, LLC (Indianapolis, Ind.) as Telone®. In one form inwhich pesticide composition 12 includes a fumigant, the fumigant ispresent in the range of 50%-90% by weight based on the total weight ofcapsule 10. In another form, the fumigant is present in the range of60%-80% by weight based on the total weight of capsule 10. In yetanother form, the fumigant is present in the range of 65%-75% by weightbased on the total weight of capsule 10, although other values for theweight percentage of the fumigant are contemplated.

Pesticide composition 12 may also include one or more materials orcomponents in addition to the pesticide. These components include, butare not limited to, (this is a non-exhaustive and non-mutually exclusivelist) spreaders, stickers, penetrants, buffers, sequestering agents,drift reduction agents, compatibility agents, anti-foam agents,preservation agents, cleaning agents, thickeners, cross-linking agents,and anti-foam agents. In one particular form, pesticide composition 12includes a thickener in addition to the pesticide. Examples of thesetypes of materials, include, but are limited to, a montmorillonite suchas bentonite, silica materials, guar gum, locust bean gum, carrageenam,alginates, methyl cellulose, sodium carboxymethyl cellulose (SCMC), andhydroxyethyl cellulose (HEC), just to provide a few possibilities. Inone particular aspect of this form, the thickener included in pesticidecomposition 12 is a fumed silica material that is aftertreated withdimethyldichlorosilane. One particular form of this type of thickener isavailable commercially from Evonik Industries (Esesen, Germany) asAerosil® R 972. In one form in which pesticide composition 12 includes athickener, the thickener is present in the range of 1%-6% by weightbased on the total weight of capsule 10. In another form, the thickeneris present in the range of 2%-5% by weight based on the total weight ofcapsule 10. In yet another form, the thickener is present in the rangeof 2%-4% by weight based on the total weight of capsule 10, althoughother values for the weight percentage of the thickener arecontemplated.

In another form, pesticide composition 12 includes the pesticide, and across-linking agent in addition to or in lieu of the thickener.Non-limiting examples of cross-linking agents that may be included inpesticide composition 12 include dialdehydes such as ethanedial orglyoxal. In forms in which pesticide composition 12 includes across-linking agent, it may be present in the range of 0.05%-2.0% byweight based on the total weight of pesticide composition 12. In anotherform, the cross-linking agent is present in the range of 0.1%-1.5% byweight based on the total weight of pesticide composition 12. In yetanother form, the cross-linking agent is present in the range of0.2%-1.0% by weight based on the total weight of pesticide composition12. In still another form, the cross-linking agent is present in therange of 0.2%-0.9% by weight based on the total weight of pesticidecomposition 12. In another form, the cross-linking agent is present inthe range of 0.25%-0.8% by weight based on the total weight of pesticidecomposition 12. In still another form, the cross-linking agent ispresent in the range of 0.05%-0.11% by weight based on the total weightof pesticide composition 12. In another form, the cross-linking agent ispresent in the range of 0.06%-0.10% by weight based on the total weightof pesticide composition 12. In yet another form, the cross-linkingagent is present in the range of 0.07%-0.09% by weight based on thetotal weight of pesticide composition 12, although other values for theweight percentage of the cross-linking agent are contemplated. In one ormore of these or other forms, the amount of the cross-linking agentincluded in pesticide composition 12 is selected to provide across-linking effect to the gelatin material of shell wall 14 in an areathat immediately surrounds pesticide composition 12 but does not extendthroughout the entire thickness of shell wall 14. One non-limiting formof capsule 10 having this configuration is schematically illustrated inFIG. 2. In this form, the cross-linked portion 16 of shell wall 14extends outwardly from pesticide composition 12 toward but terminateswell short of external surface 18. It should be appreciated that theoutward most extent of cross-linked portion 16 of shell wall 14 can becontrolled by adjusting the amount of the cross-linking agent includedin pesticide composition 12.

It is also contemplated that other pesticides could be included, eithersingularly or in combination, in pesticide composition 12 in addition toor in lieu of the fumigant. Non-limiting examples of such pesticidesinclude insecticides such as antibiotic insecticides, macrocycliclactone insecticides (for example, avennectin insecticides, milbemycininsecticides, and spinosyn insecticides), arsenical insecticides,botanical insecticides, carbamate insecticides (for example,benzofuranyl methylcarbamate insecticides, dimethylcarbamateinsecticides, oxime carbamate insecticides, and phenyl methylcarbamateinsecticides), diamide insecticides, desiccant insecticides,dinitrophenol insecticides, fluorine insecticides, formamidineinsecticides, inorganic insecticides, insect growth regulators (forexample, chitin synthesis inhibitors, juvenile hormone mimics, juvenilehormones, moulting hormone agonists, moulting hormones, moultinginhibitors, precocenes, and other unclassified insect growthregulators), nereistoxin analogue insecticides, nicotinoid insecticides(for example, nitroguanidine insecticides, nitromethylene insecticides,and pyridylmethylamine insecticides), organochlorine insecticides,organophosphorus insecticides, oxadiazine insecticides, oxadiazoloneinsecticides, phthalimide insecticides, pyrazole insecticides,pyrethroid insecticides, pyrimidinamine insecticides, pyrroleinsecticides, tetramic acid insecticides, tetronic acid insecticides,thiazole insecticides, thiazolidine insecticides, thiourea insecticides,urea insecticides, as well as, other unclassified insecticides.

More particular examples of insecticides include, but are not limitedto, 1abamectin, acephate, acetamiprid, acethion, acetoprole,acrinathrin, acrylonitrile, alanycarb, aldicarb, aldoxycarb, aldrin,allethrin, allosamidin, allyxycarb, alpha-cypermethrin,alpha-endosulfan, amidithion, aminocarb, amiton, amitraz, anabasine,athidathion, azadirachtin, azamethiphos, azinphos-ethyl,azinphos-methyl, azothoate, barium hexafluorosilicate, barthrin,bendiocarb, benfuracarb, bensultap, beta-cyfluthrin, beta-cypermethrin,bifenthrin, bioallethrin, bioethanomethrin, biopermethrin,bioresmethrin, bistrifluron, borax, boric acid, boric acid,bromfenvinfos, bromocyclen, bromo-DDT, bromophos, bromophos-ethyl,bufencarb, buprofezin, butacarb, butathiofos, butocarboxim, butonate,butoxycarboxim, cadusafos, calcium arsenate, calcium polysulfide,camphechlor, carbanolate, carbaryl, carbofuran, carbon disulfide, carbontetrachloride, carbophenothion, carbosulfan, cartap,chlorantraniliprole, chlorbicyclen, chlordane, chlordecone,chlordimeform, chlorethoxyfos, chlorfenapyr, chlorfenvinphos,chlorfluazuron, chlormephos, chloroform, chloropicrin, chlorphoxim,chlorprazophos, chlorpyrifos, chlorpyrifos-methyl, chlorthiophos,chromafenozide, cinerin I, cinerin II, cismethrin, cloethocarb,closantel, clothianidin, copper acetoarsenite, copper arsenate, coppernaphthenate, copper oleate, coumaphos, coumithoate, crotamiton,crotoxyphos, crufomate, cryolite, cyanofenphos, cyanophos, cyanthoate,cyclethrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin,cyphenothrin, cyromazine, cythioate, DDT, decarbofuran, deltamethrin,demephion, demephion-O, demephion-S, demeton, demeton-methyl, demeton-O,demeton-O-methyl, demeton-S, demeton-S-methyl, demeton-S-methylsulphon,diafenthiuron, dialifos, diatomaceous earth, diazinon, dicapthon,dichlofenthion, dichlorvos, dicresyl, dicrotophos, dicyclanil, dieldrin,diflubenzuron, dilor, dimefluthrin, dimefox, dimetan, dimethoate,dimethrin, dimethylvinphos, dimetilan, dinex, dinoprop, dinosam,dinotefuran, diofenolan, dioxabenzofos, dioxacarb, dioxathion,disulfoton, dithicrofos, d-limonene, DNOC, doramectin, ecdysterone,emamectin, EMPC, empenthrin, endosulfan, endothion, endrin, EPN,epofenonane, eprinomectin, esfenvalerate, etaphos, ethiofencarb, ethion,ethiprole, ethoate-methyl, ethoprophos, ethyl formate, ethyl-DDD,ethylene dichloride, ethylene oxide, etofenprox, etrimfos, EXD, famphur,fenamiphos, fenazaflor, fenchlorphos, fenethacarb, fenfluthrin,fenitrothion, fenobucarb, fenoxacrim, fenoxycarb, fenpirithrin,fenpropathrin, fensulfothion, fenthion, fenthion-ethyl, fenvalerate,fipronil, flonicamid, flubendiamide, flucofuron, flucycloxuron,flucythrinate, flufenerim, flufenoxuron, flufenprox, fluvalinate,fonofos, formetanate, formothion, formparanate, fosmethilan, fospirate,fosthietan, furathiocarb, furethrin, gamma-cyhalothrin, gamma-HCH,halfenprox, halofenozide, HCH, HEOD, heptachlor, heptenophos,heterophos, hexaflumuron, HHDN, hydramethylnon, hydrogen cyanide,hydroprene, hyquincarb, imidacloprid, imiprothrin, indoxacarb,iodomethane, IPSP, isazofos, isobenzan, isocarbophos, isodrin,isofenphos, isoprocarb, isoprothiolane, isothioate, isoxathion,ivermectin, jasmolin I, jasmolin II, jodfenphos, juvenile hormone 1,juvenile hormone II, juvenile hormone III, kelevan, kinoprene,lambda-cyhalothrin, lead arsenate, lepimectin, leptophos, lindane,lirimfos, lufenuron, lythidathion, malathion, malonoben, mazidox,mecarbam, mecarphon, menazon, mephosfolan, mercurous chloride,mesulfenfos, metaflumizone, methacrifos, methamidophos, methidathion,methiocarb, methocrotophos, methomyl, methoprene, methoxychlor,methoxyfenozide, methylchloroform, methylene chloride, metofluthrin,metolcarb, metoxadiazone, mevinphos, mexacarbate, milbemectin,milbemycin oxime, mipafox, mirex, monocrotophos, morphothion,moxidectin, naftalofos, naled, naphthalene, nicotine, nifluridide,nitenpyram, nithiazine, nitrilacarb, novaluron, noviflumuron, omethoate,oxamyl, oxydemeton-methyl, oxydeprofos, oxydisulfoton,para-dichlorobenzene, parathion, parathion-methyl, penfluron,pentachlorophenol, permethrin, phenkapton, phenothrin, phenthoate,phorate, phosalone, phosfolan, phosmet, phosnichlor, phosphamidon,phosphine, phoxim, phoxim-methyl, pirimetaphos, pirimicarb,pirimiphos-ethyl, pirimiphos-methyl, potassium arsenite, potassiumthiocyanate, pp′-DDT, prallethrin, precocene I, precocene II, precoceneIII, primidophos, profenofos, profluthrin, promacyl, promecarb,propaphos, propetamphos, propoxur, prothidathion, prothiofos, prothoate,protrifenbute, pyraclofos, pyrafluprole, pyrazophos, pyresmethrin,pyrethrin I, pyrethrin II, pyridaben, pyridalyl, pyridaphenthion,pyrifluquinazon, pyrimidifen, pyrimitate, pyriprole, pyriproxyfen,quassia, quinalphos, quinalphos-methyl, quinothion, rafoxanide,resmethrin, rotenone, ryania, sabadilla, schradan, selamectin,silafluofen, silica gel, sodium arsenite, sodium fluoride, sodiumhexafluorosilicate, sodium thiocyanate, sophamide, spinetoram, spinosad,spiromesifen, spirotetramat, sulcofuron, sulfluramid, sulfotep, sulfurylfluoride, sulprofos, tau-fluvalinate, tazimcarb, TDE, tebufenozide,tebufenpyrad, tebupirimfos, teflubenzuron, tefluthrin, temephos, TEPP,terallethrin, terbufos, tetrachloroethane, tetrachlorvinphos,tetramethrin, theta-cypermethrin, thiacloprid, thiamethoxam, thicrofos,thiocarboxime, thiocyclam, thiodicarb, thiofanox, thiometon, thiosultap,thuringiensin, tolfenpyrad, tralomethrin, transfluthrin,transpermethrin, triarathene, triazamate, triazophos, trichlorfon,trichlormetaphos-3, trichloronat, trifenofos, triflumuron, trimethacarb,triprene, vamidothion, vaniliprole, XMC, xylylcarb, zeta-cypermethrin,zolaprofos, and α-ecdysone.

For more information consult “COMPENDIUM OF PESTICIDE COMMON NAMES”located at http://www.alanwood.net/pesticides/index.html. Also consult“THE PESTICIDE MANUAL” 14th Edition, edited by C D S Tomlin, copyright2006 by British Crop Production Council.

As indicated above, various properties of capsule 10 can be altered tocontrol characteristics of the release of pesticide composition 12therefrom. In addition to or in lieu of modifying these properties,capsule 10 may also include a protease enzyme on its exterior surface toaccelerate degradation of capsule 10 and the resulting release ofpesticide composition 12 therefrom. Non-limiting examples of proteaseenzymes that could be included on capsule 10 include pepsin, trypsin,ficin, bromelain, papain, rennin and chymotrypsin. Variations in theacceleration of degradation of capsule 10 caused by the protease enzymecan be controlled by modifying the concentration of the enzyme. Forexample, it should be appreciated that higher enzyme concentrations willresult in faster capsule degradation and release of pesticidecomposition 12 therefrom. Similarly, time profiles of the degradation ofcapsule 10 and the resultant release of pesticide composition 12therefrom can be experimentally determined in order to facilitate thedesign of capsules 10 having release profiles tailored for particularapplications. For example, in one particular instance where release ofpesticide composition 12 from capsule 10 is desired to begin within afew hours of its application to a locus where pest control is desired,capsule 10 may be provided with a requisite amount and/or concentrationof the enzyme to achieve such release. In other forms where a greaterperiod of time is desired between the application of capsule 10 at thelocus and the initiation of release of pesticide composition 12therefrom, the amount and/or concentration of the enzyme can be modifiedas necessary.

In one form, the protease enzyme is dissolved in water to provide anenzyme solution that is applied to the external surface of capsule 10.Optional components that could be included in this solution includethickeners, stabilizers or extenders, just to provide a few non-limitingexamples. The protease enzyme may also be applied to the externalsurface of capsule 10 in a dust or powder form. Non-limiting examples ofdusts or powders in which the enzyme may be mixed include kaolin clay,ground volcanic rock, attapulgite clays, montmorillonite clays,diatomaceous earths, talc, bentonite, calcium carbonate and whitecarbon. In one particular but non-limiting form, a powder including amixture of the enzyme and lactose is applied to capsule 10. One optionalcomponent that could be included in these dusts or powders is asurfactant, although the inclusion of additional components is alsocontemplated.

Capsule 10 may be formed utilizing any conventional encapsulationtechnique known in the art including, by way of non-limiting example, arotary die encapsulation process. In this process, the materials formingshell wall 14 are provided as a heated, flowable mixture that isdeposited on opposite cooling drums to form separate ribbons. Theseribbons are conveyed to an injection wedge by a series of rollers, andthe injection wedge guides the ribbons between a pair of oppositelypositioned die rolls which couple the ribbons together to form acapsule. Before the ribbons are entirely coupled, the pesticidecomposition is injected therebetween by the injection wedge. Afterformation, the capsules may further undergo a drying step. Depending onthe materials used in connection with capsule 10, regular maintenance ofthe rotary die apparatus may be necessary to avoid corrosion of variousworking surfaces, moving parts, or other components. For example, in oneform in which 1,3-dichloropropene is included in pesticide composition12, it may be necessary to ensure that various lubricating materials areregularly changed in order to avoid corrosion.

The locus to which capsule 10 may be applied can be any locus inhabitedby a pest including, for example, vegetable crops, fruit and nut trees,grape vines, ornamental plants, domesticated animals, the interior orexterior surfaces of buildings, and the soil around buildings.Controlling pests generally means that pest populations, activity, orboth, are reduced in a locus. This can come about when: pest populationsare repulsed from a locus; when pests are incapacitated in or around alocus; or pests are exterminated, in whole or in part, in or around alocus. Of course a combination of these results can occur.

In one particular application, capsule 10 is placed on the surface ofsoil or buried in the soil. In either case, capsule 10 may be positionedutilizing a variety of different techniques. For example, when it isapplied on the surface of soil, capsule 10 may be hand placed ordispersed with a broadcast or other type of mechanical spreader.Non-limiting burial techniques include the formation of trenches, holes,or other openings in the soil in which one or more capsules 10 areplaced and then covered by soil. The particular spacing and depth atwhich capsule 10 is buried may depend on a variety of factors, includingfor example, soil type, targeted pests, and degree of infestation.

At some time after burial, shell wall 14 of capsule 10 will graduallydegrade by, for example, breaking apart or fracturing as a result ofswelling. When present, the enzyme on capsule 10 also causes itsdegradation. Upon gradual degradation of capsule 10, the resultantrelease of pesticide composition 12 from capsule 10 is also gradual.However, forms in which the degradation of capsule 10 and the release ofpesticide composition 12 therefrom are more sudden are also possible.When pesticide composition 12 includes a fumigant in a liquid form forexample, it will vaporize and penetrate the soil surrounding theoriginal burial location of capsule 10 after being released therefrom.It should be understood that the length of time required for pesticidecomposition 12 to be released from capsule 10 following its burial willdepend on a variety of factors, including for example, the physicalproperties of capsule 10 and/or the temperature, moisture, and pH of thesoil. The length of time required for pesticide composition 12 to bereleased from capsule 10 following its burial will also depend, whereapplicable, on the amount and/or concentration of the enzyme provided oncapsule 10. In certain forms, including those where capsule 10 includesan enzyme, it may be desirable to irrigate the soil where capsule 10 hasbeen positioned in order to increase its moisture content for promotingdegradation of capsule 10. For example, in some instances the soil canbe irrigated until a moisture content in the range of 20%-40% of thesoil is achieved.

EXAMPLES

The examples are for illustration purposes and are not to be construedas limiting the invention disclosed in this document to only theembodiments disclosed in these examples.

Example I Capsule Production

A capsule fill mixture was prepared by adding 0.48 kg of Aerosil® R 972(Evonik Industries, Essen, Germany) to 11.6 kg of 1,3-dichloropropeneusing moderate agitation. Agitation was continued taking care to avoiddrawing air into the mixture until it was homogeneous (approximately 10minutes).

A capsule shell material was prepared by first heating 8.7 kg of waterand 2.6 Kg of Sorbitol Special™ (SPI Pharma, Wilmington, Del.) to 70° C.in a jacketed vessel and then adding 8.7 kg of 270 bloom type B gelatin(270 Bloom Lime Bone Gelatin, ZA-B270-2, Eastman Gelatine, Peabody,Mass.) to it with sufficient agitation to completely wet the gelatin.

Care was taken to avoid drawing air into the mixture or otherwisecreating foam. After the gelatin was wetted, the batch temperature wasreduced to 60° C. and a vacuum drawn on the vessel to de-aerate thematerial. When de-aerated, the gelatin was a clear, dark caramel color.

The 1,3-dichloropropene-Aerosil® R 972 mixture was encapsulated using anR&D 4″ Softgel Pilot Plant (CapPlus Technologies, Phoenix, Ariz.) fittedwith #20 round dies to produce 1 ml capsules (12.7 mm diameterspherical) or #40 dies to produce 2 ml capsules (15.7 mm diameterspherical). The chill rolls on the encapsulator were set to 18-20° C.and the gap between the spreader box and chill roll was set to 0.9 mm.The spreader box temperature was set to 60° C. and the wedge temperaturewas set to 39-41° C. or the temperature required for the particulargelatin in use to create a successful seal. The encapsulation machinewas operated at a speed of 4.5 rpm, equivalent to 20 liters/hour of1,3-dichloropropene-Aerosil® R 972 mixture feed and approximately 6liters per hour of gelatin-sorbitol-water mixture feed. The gel capsulesproduced were dried in a tumble dryer for 15 minutes and thentransferred to trays for air drying for 24 to 48 hours. Encapsulationand drying were done at an ambient temperature of 18-21° C. and 30-35%relative humidity. The composition of the produced gel capsules isprovided in Table 1:

TABLE 1 Component Component Wt % 1,3-dichloropropene 72.95 gelatin 15.07Sorbitol Special ™ 4.68 epoxidized soybean 1.12 oil Aerosil ® R 972 3.14impurities from tech. 1.21 water 1.83

Example II Determination of 1,3-Dichloropropene Loss from Capsules

Gel capsules from Example I above (capsules A) were compared to gelcapsules having a wall made from 150-200 low-bloom gelatin (capsules B)with respect to 1,3-dichloropropene (1,3-D) lost therefrom. Each ofcapsules A and B had a 1 mL volume and was in the form of a 12.7 mmdiameter sphere. Capsules A and B were placed in 10 mL size glass vials(one capsule/vial) and sealed with crimp tight caps. The vials werestored at room temperature or at 40° C. for the times indicated in Table2.

The head space in each vial was then analyzed by using a gas tightsyringe to take a 500 microliter sized sample and injecting the sampleinto a Model HP6890 gas chromatograph equipped with a 25 meter DB-5MScolumn (25 mm×0.52 um) and an FID detector. The amount ofcis/trans-1,3-dichloropropene in each injected sample was measured asthe peak area counts from the FID detector and was compared to relevantstandard samples to determine the amount of 1,3-D in the headspace(amount lost from the capsule). The results are provided in Table 2.

TABLE 2 1,3-D Lost Headspace From Capsule Peak Area Relative to GelStorage Counts Initial Capsule Gel Capsule Core Conditions (cis + trans)(% wt/wt) A 1,3-D/Aerosil ®  5 days @ 0 0 R 972 room temp A1,3-D/Aerosil ®  5 days @ 734 0.007 R 972 40° C. A 1,3-D/Aerosil ® 10days @ 0 0 R 972 room temp A 1,3-D/Aerosil ® 10 days @ 19732 0.2 R 97240° C. B 1,3-D  2 days @ 240516 2.45 room temp B 1,3-D  7 days @ 4228164.32 room temp B 1,3-D  7 days @ 1624012 16.57 40° C.

Example III Capsule Field Trials

Field trials for the gel capsules of Example I were established undercommercial conditions in banana production areas of Central America.Bananas were transplanted using commercial procedures typical of thearea. Gel capsules according to Example I were used as a post-planttreatment. A commercial standard was also included as a comparison ineach test. Treatments and use rates for both field trials are includedin the Tables 3 and 4 below. Location 1 included four replications foreach treatment and location 2 included three replications.

TABLE 3 Location 1 Treatment Pesticide Use number Pesticide TreatmentFormulation rate 1 1,3-dichloropropene 1 mL gel caps 5 L/Ha 21,3-dichloropropene 1 mL gel caps 10 L/Ha 3 1,3-dichloropropene 1 mL gelcaps 15 L/Ha 4 1,3-dichloropropene 1 mL gel caps 20 L/Ha 5 fenamiphos¹Granules 5 Kg/Ha ¹Fenamiphos was supplied as Nemacur 15 G (Bayer)

TABLE 4 Location 2 Treatment Pesticide Use number Pesticide TreatmentFormulation rate 1 1,3-dichloropropene 1 mL gel caps 5 L/Ha 21,3-dichloropropene 1 mL gel caps 10 L/Ha 3 1,3-dichloropropene 1 mL gelcaps 15 L/Ha 4 1,3-dichloropropene 1 mL gel caps 20 L/Ha 5 cadusafos¹Granules 3.5 Kg/Ha ¹Cadusafos was supplied as Rugby 10 G (FMCCorporation)

Gel caps were applied in the area immediately surrounding the base ofthe banana plant. Holes were made to a depth of 15-20 cm using a rodinserted into the soil. Gel caps were applied into the holes by hand andsoil was reapplied into the holes to cover the gel caps. Commercialstandards were formulated as granules and applied around the base of theplant without incorporation.

Several parameters were measured at intervals following application ofthe pesticide. Plant height and plant trunk diameter were evaluated overtime at intervals of approximately two, four and six weeks afterapplication of the pesticide. Root weight, percent functional roots andnematode counts were taken at intervals of 45 and 60 days afterapplication (DAA). Plant height and trunk diameter were evaluated asdirect measurements and are recorded in units of centimeters. Rootweight, percent functional roots and nematode counts were obtained byseparate soil samples which were taken and returned to the lab foranalysis. Roots were separated from the soil and weighed. A separate,visual estimate was made to determine the percent of these roots thatwere healthy and functional. Nematode counts were made by extractingthem from the roots and soil and then estimating the total by countingthe actual number in subsamples of the extracted materials.

Trends in most parameters measured were similar between the 1,3-D gelcap treatments and the commercial standard when measured over theevaluation periods (results shown in Tables 5 and 6). Most parametersshowed an improvement over time. The overall conclusion is that 1,3-Dapplied via gel capsules according to Example I provides resultscomparable to commercial standards in both trial locations and was aviable alternative to existing commercial treatments.

TABLE 5 Treatment and Rate Growth Evaluation 1,3-D @ 1,3-D @ 1,3-D @1,3-D @ fenamiphos Parameter Time (DAA) 5 L/Ha 10 L/Ha 15 L/Ha 20 L/Ha @5 Kg/Ha Plant 14 164  176  173  174  162  Height 28 172  183  190  180 173  (cm) 42 182  191  201  190  182  Root 45 86 78 46 54 64 weight 6048 68 34 47 46 Stem 14 34 36 36 34 34 diameter 28 38 40 41 38 37 (cm) 4242 44 44 42 41 Nematode 45 21,750a   25,650a   20,950a   17,100a  14,800a   count 60 38,400a   30,400a   40,150a   40,400a   26,500a   %Functional 45 80 71 66 65 73 roots 60 83 83 72 67 83

TABLE 6 Treatment and Rate Growth Evaluation 1,3-D @ 1,3-D @ 1,3-D @1,3-D @ cadusaphos Parameter Time (DAA) 5 L/Ha 10 L/Ha 15 L/Ha 20 L/Ha @3.5 Kg/Ha Plant 15 143  150  147  145  143  Height 29 152  161  158 156  156  (cm) 43 161  168  169  165  169  Root 45 43 47 42 52 44 weight(gms) 60 74 61 37 75 53 Stem 15 30 31 31 31 30 diameter 29 33 34 35 3433 (cm) 43 35 37 37 36 36 Nematode 45 18,133a   25,333a   24,800a  20,533a   11,200a   count 60 17,200a   22,400a   18,933a   25,200a  23,733a   % Functional 45 83 80 86 74 82 roots 60 81 84 81 91 86

Example IV Cross-Linked Capsules—Preparation and Composition

Using the components and amounts shown in Table 7, gelatin capsules wereprepared using various amounts of the gelatin cross-linking agentglyoxal. 1,3-dichloropropene (technical grade) was combined withAerosil® R972 (Evonik Industries, Essen, Germany) under continuousagitation to form a smooth, homogeneous mixture with no entrained air.Glyoxal was combined with emulsifier Atlox™ 4851B (Croda Crop Care,Cowick Hall, East Yorkshire, England) and added to the1,3-dichloropropene/Aerosil R972 mixture to form the pesticidecomposition as an emulsion. Pesticide composition samples were preparedwith glyoxal concentrations of 0.0 (control) 0.25, 0.5 and 0.8% byweight.

The capsule shell material was prepared by first heating 7.24 kg ofwater and 3.16 Kg of Sorbitol Special™ (SPI Pharma, Wilmington, Del.) to70° C. in a jacketed vessel and then adding 8.0 kg of 270 bloom type Bgelatin (270 Bloom Lime Bone Gelatin, ZA-B270-2, Eastman Gelatine,Peabody, Mass.) to it with sufficient agitation to completely wet thegelatin. Care was taken to avoid drawing air into the mixture orotherwise creating foam. After the gelatin was wetted, the batchtemperature was reduced to 60° C. and a vacuum drawn on the vessel tode-aerate the material. When de-aerated, the gelatin was a clear, darkcaramel color.

The 1,3-dichloropropene/Aerosil® R972/glyoxal mixtures were eachencapsulated with the gelatin prepared herein using the equipment andmethod described in Example Ito produce 1 ml volume capsules. Each ofthe pesticide composition samples containing 0.0, 0.25, 0.5 and 0.8weight % of glyoxal used to fill the gel capsules were fed sequentiallywith a sufficient transition time to allow the equipment to be clearedbefore starting a new concentration. The gel capsules produced were nottumble dried, but were immediately transferred to trays for air dryingfor 24 to 48 hours. Encapsulation and drying were done at an ambienttemperature of 18-21° C. and 30-35% relative humidity.

TABLE 7 Gel Capsules Prepared with Glyoxal Cross-linker Sample Number 2A2C 2D 2E Glyoxal in Pesticide Composition (before encapsulation, wt %)0.00 0.25 0.50 0.80 Gel Capsule Composition Component (wt %) After AirDrying 1,3-Dichloropropene 72.27 72.09 71.91 71.69 (tech. grade) Atlox ™4851B 3.01 3.00 3.00 2.99 Glyoxal 0.00 0.20 0.39 0.63 Aerosil ® R9723.14 3.13 3.12 3.11 Gelatin 15.07 15.07 15.07 15.07 Sorbitol Special ™4.68 4.68 4.68 4.68 Water (residual) 1.83 1.83 1.83 1.83 Total 100.00100.00 100.00 100.00

Cross-Linked Capsules—Storage Stability

The gel capsules prepared with varying amounts of glyoxal cross-linker(0.00, 0.25, 0.50 and 0.80 wt%) in the pesticide composition (Table 7)were stored at 65° C. for 72 hours in 10 mL glass vials and were thenanalyzed for the loss of 1,3-dichloropropene from the gel capsule intothe headspace of the vial as described in Example II. Three replicationsof each sample were analyzed and the Grubbs test (Grubbs, F. E., “Samplecriteria for testing outlying observations,” Annals of MathematicalStatistics, 21 (1950); Grubbs, F., “Procedures for detecting OutlyingObservations in Samples,” Technometrics, 11/1, 1-21 (1969)) was used toremove any statistical outliers from the data collected.

FIG. 3 shows the loss of 1,3-dichloropropene from the four types of gelcapsules based on the GC area counts of a 500 microliter sample removedfrom the headspace of each storage vial. All three gel capsule samplesprepared with glyoxal cross-linker showed a 97.8 to 99.0% reduction inthe loss of 1,3-dichloropropene when compared to the control sample 2A.

Example V Release of 1,3-Dichloropropene from Gel Capsules Placed inSoil

The following 1,3-dichloropropene samples shown in Table 8 were used ina soil release study described herein. Samples 2A and 2C were preparedas described in Example IV. Sample 2C-P was prepared by placing one gelcapsule 2C in a 30 mL vial and adding 25 mg of papain enzyme to it. Thepapain enzyme was obtained from Biocatalysts, Batch #2485211. Thecapsule was gently agitated in the enzyme until evenly coated.

TABLE 8 Sample Composition Source Control 1 mL liquid 1,3- Supelco LotLB73623, purity dichloropropene 99.9%; cis/trans 50.6/49.3 2A 1 mL gelcapsule Example IV 2C 1 mL gel capsule cross-linked Example IV with0.25% glyoxal 2C-P 1 mL gel capsule cross-linked with 0.25% glyoxal andcoated Example IV-V with papain enzyme

Soil and Soil Column Preparation

The soil was prepared by taking prescreened sandy loam soil and addingapproximately 10 mL of water per 100 g of soil. The soil was placed in 6inch tall by 4.25 inch wide cylindrical glass containers with one endsealed. Soil was placed in the glass containers to within approximately1 inch from the top of the vessels. Finally, the 1,3-dichloropropenesamples were applied to the soil in the containers by creating a hole inthe center of the soil column and placing the sample at approximatelyhalf of the depth of the soil column. The samples were then covered withmoistened soil.

Release of 1,3-Dichloropropene from Soil Columns

The release study was conducted by placing a soil column in an apparatusand flowing metered air at 1 liter/min across the top of the system andcapturing the released 1,3-dichloropropene in activated carbon capturetubes. SKC air check samplers (SKC, Inc., Eighty Four, Pa., Model224-PCXR8) were used to pull air through the carbon capture tubes. Theair flow was metered across the carbon capture tubes in order to accountfor any loss of pressure resulting from restriction by the carboncapture tube. Anasorb® CSC (SKC, Inc., Eighty Four, Pa.) sample tubescontaining coconut charcoal sorbent (catalog #226-16, 10×110 mm; 2sections; 200+800 mg of sorbent; foam, glass wool & glass woolseparators) were used to capture the volatilized 1,3-dicloropropene. Thesoil release study was conducted over a two week time period. Uponcompletion, the carbon capture tubes were extracted with 10 mL of hexaneby use of a shaker for approximately 1 hour. An aliquot of the hexaneextract was then analyzed by GC/MS.

The release profiles of the three 1,3-dichloropropene gel capsules andthe liquid 1,3-dichloropropene control sample are shown in FIG. 4. Allthree of the gel capsules exhibited slower release of1,3-dichloropropene compared to the liquid 1,3-dichloropropene controlsample. Additionally, the papain enzyme coated gel capsule showed fasterrelease of 1,3-dichloropropene compared to either of the other gelcapsules.

In one embodiment, a capsule includes a shell wall encapsulating apesticide composition and including a gelatin material having a Bloomstrength in the range of 250 to 300 grams and a plasticizer composition.The gelatin material and the plasticizer composition are present at aratio by weight between 2:1 and 4:1. In one form of this embodiment, theplasticizer composition includes a mixture of sorbitol and mannitol. Inone aspect of this form, the mixture further includes sorbitolanhydrides. In another form of this embodiment, the gelatin material andthe plasticizer composition are present at a weight ratio between 3:1and 3.5:1. In still another form of this embodiment, the pesticidecomposition includes a fumigant. In one aspect of this form, thefumigant is 1,3-dichloropropene. In another aspect of this form, thepesticide composition further includes a fumed silica material. In afurther aspect, the fumed silica material is hydrophobic andaftertreated with dimethyldichlorosilane. In yet another aspect of thisform, the pesticide composition further includes a cross-linking agent.In a further aspect, the cross-linking agent is a dialdehyde. In an evenfurther aspect, the dialdehyde is ethanedial. In still another aspect,the cross-linking agent is present in the range of 0.06% to 0.1% byweight based on total weight of the pesticide composition. In anotherform of this embodiment, the capsule the capsule further includes aprotease enzyme. In one aspect of this form, the protease enzyme is acomponent of a powder mixture further including lactose. In anotheraspect of this form, the protease enzyme is selected from papain andbromelain.

In another embodiment, a capsule includes a shell wall including agelatin material and a plasticizer composition that includes a mixtureof sorbitol and mannitol. The capsule also includes a pesticidecomposition encapsulated by the shell wall, and the pesticidecomposition includes a fumigant and a fumed silica material. In one formof this embodiment, the gelatin material has a Bloom strength in therange of 250 to 300 grams. In another form of this embodiment, thegelatin material and the plasticizer composition are present at a ratioby weight between 2:1 and 4:1. In still another form of this embodiment,the mixture further comprises sorbitol anhydrides. In yet another formof this embodiment, the fumigant is 1,3-dichloropropene. In another formof this embodiment, the fumed silica material is hydrophobic andaftertreated with dimethyldichlorosilane. In still another form of thisembodiment, the pesticide composition further includes a cross-linkingagent. In one aspect of this form, the cross-linking agent is adialdehyde. In a further aspect, the dialdehyde is ethanedial. Inanother form of this embodiment, the capsule further includes a proteaseenzyme. In one aspect of this form, the protease enzyme is a componentof a powder mixture further including lactose. In another aspect of thisform, the protease enzyme is selected from papain and bromelain.

In yet another embodiment, a capsule includes a shell wall formed by agelatin composition and encapsulating a pesticide composition. Thepesticide composition includes a fumigant, a fumed silica material and adialdehyde cross-linking agent. In one form of this embodiment, thefumed silica material is hydrophobic and aftertreated withdimethyldichlorosilane. In another form of this embodiment, thedialdehyde cross-linking agent is ethanedial. In still another form ofthis embodiment, the cross-linking agent is present in the range of0.06% to 0.1% by weight based on total weight of the pesticidecomposition. In yet another form of this embodiment, the capsule furtherincludes a protease enzyme selected from papain and bromelain. Inanother form of this embodiment, the gelatin composition includes type-Bgelatin and a plasticizer including a mixture of sorbitol, mannitol andsorbitol anhydrides. In yet another form, the fumigant is1,3-dichloropropene.

In still another embodiment, a process includes providing a firstmixture including a fumed silica material and 1,3-dichloropropene;providing a second mixture including type-B gelatin and a plasticizerincluding a mixture of sorbitol, mannitol and sorbitol anhydrides; andencapsulating the first mixture in the second mixture using a rotary dieapparatus.

Other embodiments includes methods or techniques involving the placementof one or more capsules at a locus where pest control is desired.

The headings in this document are for convenience only and must not beused to interpret any portion thereof.

While the invention has been illustrated and described in detail in thedrawings and foregoing description, the same is to be considered asillustrative and not restrictive in character, it being understood thatonly certain embodiments have been shown and described and that allchanges and modifications that come within the spirit of the inventionsare desired to be protected. It should be understood that while the useof words such as preferable, preferably, preferred or more preferredutilized in the description above indicate that the feature so describedmay be more desirable, it nonetheless may not be necessary andembodiments lacking the same may be contemplated as within the scope ofthe invention, the scope being defined by the claims that follow. Inreading the claims, it is intended that when words such as “a,” “an,”“at least one,” or “at least one portion” are used there is no intentionto limit the claim to only one item unless specifically stated to thecontrary in the claim. When the language “at least a portion” and/or “aportion” is used the item can include a portion and/or the entire itemunless specifically stated to the contrary.

What is claimed is:
 1. A capsule, comprising a shell wall encapsulatinga pesticide composition and including a gelatin having a Bloom strengthin the range of 270 to 300 grams, wherein the pesticide compositionincludes 1,3-dichloropropene.
 2. The capsule of claim 1, wherein theshell wall further includes a plasticizer composition.
 3. The capsule ofclaim 2, wherein the plasticizer composition includes a mixture ofsorbitol and mannitol.
 4. The capsule of claim 1, wherein the pesticidecomposition further includes a cross-linking agent.
 5. The capsule ofclaim 4, wherein the cross-linking agent is a dialdehyde.
 6. The capsuleof claim 5, wherein the dialdehyde is ethanedial.
 7. The capsule ofclaim 4, wherein the cross-linking agent is present in the range of0.06% to 0.1% by weight based on total weight of the pesticidecomposition.
 8. The capsule of claim 1, further comprising a proteaseenzyme.
 9. The capsule of claim 8, wherein the protease enzyme isselected from papain and bromelain.
 10. The capsule of claim 1, furthercomprising a mixture of a protease enzyme and lactose.
 11. A capsule,comprising a shell wall formed by a gelatin composition including agelatin having a Bloom strength in the range of 270 to 300 grams, theshell wall encapsulating a pesticide composition including1,3-dichloropropene, a fumed silica material and a dialdehydecross-linking agent.
 12. The capsule of claim 11, wherein the fumedsilica material is hydrophobic and aftertreated withdimethyldichlorosilane.
 13. The capsule of claim 11, wherein thedialdehyde cross-linking agent is ethanedial.
 14. The capsule of claim11, wherein the gelatin composition includes a mixture of sorbitol,mannitol and sorbitol anhydrides.
 15. A process, comprising: providing afirst composition including 1,3-dichloropropene; providing a secondcomposition including a gelatin having a Bloom strength in the range of270 to 300 grams; and encapsulating the first composition in the secondcomposition using a rotary die apparatus.
 16. The process of claim 15,wherein the first composition further includes a fumed silica materialand a glyoxal cross-linking agent.
 17. The process of claim 15, whereinthe second composition further includes a mixture of sorbitol, mannitoland sorbitol anhydrides.
 18. A method, comprising: identifying a locuswhere pest control is desired; and positioning one or more capsules atthe locus, the capsules including a shell wall encapsulating1,3-dichloropropene and including a gelatin having a Bloom strength inthe range of 270 to 300 grams.
 19. The method of claim 18, wherein thepositioning includes at least one of placing the one or more capsules ona surface of soil at the locus and burying the one or more capsules inthe soil at the locus.